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Structure of 1206979-75-0
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6-Chloro-1H-pyrazolo[4,3-c]pyridin-3-amine delivers a rigid, electron-deficient heterocyclic scaffold ideal for medicinal chemistry. This bench-stable compound integrates readily into kinase inhibitor scaffolds and engages in efficient cross-coupling reactions. The chloro group enables further functionalization, while the pyrazolopyridine core supports hydrogen bonding interactions in target binding.
6-Chloro-1H-pyrazolo[4,3-c]pyridin-3-amine serves as a versatile building block for medicinal chemistry and heterocyclic synthesis. The chloro group enables palladium-catalyzed cross-coupling reactions, while the primary amine facilitates derivatization via acylation, alkylation, or Ullmann-type coupling. This scaffold exhibits excellent bench stability and compatibility with common protecting group strategies, making it ideal for iterative synthesis of kinase inhibitors and other bioactive molecules.
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GHS Pictogram :
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GHS No : GHS07
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Signal Word : Warning
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UN#: N/A
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Class : N/A
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Packing Group : N/A
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Hazard Statements : H302-H315-H319-H335
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Precautionary Statements : P261-P264-P270-P271-P280-P302+P352-P304+P340-P305+P351+P338-P330-P362+P364-P403+P233-P405-P501
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Lot numbers can be found on the outside label of a product: